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Characterization of SETD1A haploinsufficiency in humans a... | ResearchHub
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Characterization of SETD1A haploinsufficiency in humans and Drosophila defines a novel neurodevelopmental syndrome.
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Authors
Joost Kummeling
44 more
Joost Kummeling
•
Martin Higgs
42 more
•
Tjitske Kleefstra
Published
December 18, 2019
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Topics
Biology
Genetics And Genomics
Genetics
Haploinsufficiency
Microcephaly
Show all topics
DOI
10.1101/2019.12.17.879189
License
CC-BY-ND
Other Formats
PDF
Supporters
Support the authors with ResearchCoin
Tip RSC
Preprint Server
Topics
Biology
Genetics And Genomics
Genetics
Haploinsufficiency
Microcephaly
Show all topics
DOI
10.1101/2019.12.17.879189
License
CC-BY-ND
Other Formats
PDF
